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(3aS,4R,6S,6aR,E)-4-[2-(4-trifluoromethyl-phenyl)-vinyl]-6-vinyl-tetrahydro-cyclopenta[c]furan-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1235239-64-1

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1235239-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235239-64-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,2,3 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1235239-64:
(9*1)+(8*2)+(7*3)+(6*5)+(5*2)+(4*3)+(3*9)+(2*6)+(1*4)=141
141 % 10 = 1
So 1235239-64-1 is a valid CAS Registry Number.

1235239-64-1Downstream Products

1235239-64-1Relevant academic research and scientific papers

Optically Pure C1-Symmetric Cyclic(alkyl)(amino)carbene Ruthenium Complexes for Asymmetric Olefin Metathesis

Bertrand, Guy,Cavallo, Luigi,Crévisy, Christophe,Dorcet, Vincent,Falivene, Laura,Jazzar, Rodolphe,Mauduit, Marc,Morvan, Jennifer,Roisnel, Thierry,Vanthuyne, Nicolas,Vermersch, Fran?ois,Vives, Thomas,Zhang, Ziyun

, p. 19895 - 19901 (2020)

An expedient access to the first optically pure ruthenium complexes containing C1-symmetric cyclic (alkyl)(amino)carbene ligands is reported. They demonstrate excellent catalytic performances in asymmetric olefin metathesis with high enantioselectivities (up to 92% ee). Preliminary mechanistic insights provided by density functional theory models highlight the origin of the enantioselectivity.

Highly active chiral ruthenium-based metathesis catalysts through a monosubstitution in the N-heterocyclic carbene

Tiede, Sascha,Berger, Anke,Schlesiger, David,Rost, Daniel,Luehl, Anja,Blechert, Siegfried

supporting information; experimental part, p. 3972 - 3975 (2010/09/03)

(Chemical Equotion Present) Single (substitution) is better: New chiral ruthenium metathesis (pre)catalysts with a monosubstituted carbon atom in the N-heterocyclic carbene ligand are highly stable in solution, initiate easily, show very high enantioselectivity and excellent E selectivity in asymmetric ring-opening cross-metathesis (see scheme).

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